Drying process

ABSTRACT

The present invention relates to a method of drying biological and other labile samples so that they can be preserved as a highly viscous liquid. The method involves the steps of preparing a preservation sample by dissolving/suspending an active agent in a solution of a stabilizing agent, subjecting the preservation sample to such temperature and pressure conditions that the preservation sample loses solvent by evaporation without freezing or bubbling to form a foam and removing solvent until the preservation sample dries to form a highly viscous liquid.

This application is a 371 of International Application No.PCT/EP2003/012191, filed 30 Oct. 2003.

The present invention relates to the preservation of biological andother labile samples, to such preserved samples and to a novel processfor preserving such samples. The novel process comprises adding a sampleincluding an active agent and a stabilizing agent to a container,subjecting the sample to such temperature and pressure conditions tocause solvent loss by evaporation without freezing the sample orbubbling to form a foam. Subsequently, during a secondary drying phase,pressure and temperature conditions are maintained or adjusted so thatsolvent is removed and the preservation sample dries to form a highlyviscous liquid. Further provided by the present invention arecompositions preserved by the process of the present invention and inparticular preserved vaccine compositions.

There is a need to extend the stability and thus the shelf life oflabile samples, particularly biological samples. Traditionally, this hasbeen accomplished using the process of freeze drying in which a solutionof the substance is made and the sample is frozen. During the primarydrying phase, most of the water is removed by sublimation from ice underreduced pressure conditions and a porous ‘cake’ is formed. This isusually followed by a secondary drying phase when the pressure andtemperature are changed and water is evaporated from the solid ‘cake’.The resulting lyophilized sample has improved stability compared to aliquid formulation. However, the freeze drying process is lengthy,expensive and can be the rate limiting step in a production process.

Freeze drying can also lead to the loss of activity or antigenicity ofsome active agents. For certain biological materials such as live virus,there can be significant loss of activity during the freeze dryingprocess (Pikal (1994) ACS Symposium 567: 120-133). Many freeze driedsubstances are still unstable at ambient temperature (Carpenter et al(1994) ACS Symposium 567; 134-147).

Damage caused by the process of freezing may be circumvented to somedegree by use of stabilizing agents such as polyols. Furtherimprovements on the process of lyophilization have also been made byavoiding freezing the sample during the process and removing water byboiling (WO96/40077; U.S. Pat. No. 6,306,345). This method involvespreparing a mixture of a glass-matrix forming material in a suitablesolvent together with the sample to be preserved, evaporating bulksolvent from the mixture to obtain a syrup, exposing the syrup to apressure and temperature sufficient to cause boiling of the syrup andremoving residual solvent. Methods similar to this may be referred to asfoam drying techniques. Such techniques will expose the sample to bepreserved to stresses due to the formation and bursting of bubblesduring the ‘boiling’ stage. Especially where labile substances are to bepreserved, this may result in a loss of activity.

A similar method was described in U.S. Pat. No. 5,766,520, in which theprocess involves partially removing the water to form a viscous fluidand further subjecting the syrup to vacuum to cause it to ‘boil’ andfurther drying at temperatures substantially lower than 100° C. Thismethod still suffers from some of the problems of conventionalfreeze-drying. When the process is carried out in a large freeze-dryer,samples will dry at different rates depending on their position on theshelf and this leads to different samples loosing different amount ofactivity during the drying process. This leads to a lack of consistencywithin a batch.

Trehalose is a polyol that is favoured for its stabilizing properties.Trehalose is a naturally occurring, inert, non-reducing and non-toxic,glass-forming disaccharide that was initially found to be associatedwith the prevention of desiccation damage in some plants and animals.Trehalose is useful in preventing denaturation of a wide variety ofsubstances including proteins, viruses and foodstuffs during desiccationand subsequent storage partly because it has a relatively high glasstransition temperature (ca 120° C. in the anhydrous state) (U.S. Pat.Nos. 4,891,319; 5,149,653; 5,026,566). Trehalose also stabilizes enzymes(Argall and Smith (1993) Biochem. Mol. Biol. Int. 30; 491). Trehaloseand a wide variety of stabilizing polyols have also been found to beuseful in improving the preservation of freeze-dried samples, especiallyin cases where the sample is prone to loss of activity during thefreeze-drying process. Other sugars useful in lyophilization techniquesinclude sucrose and lactose.

The present invention relates to an improved method of preserving anactive agent, particularly if the active agent is labile and prone toloss of activity during a more conventional drying process. The processcomprises the steps of preparing a preservation sample bydissolving/suspending an active agent in a solution of a stabilizingagent; subjecting the preservation sample to such temperature andpressure conditions that the preservation sample looses solvent byevaporation, without the sample freezing or bubbling to form a foam; andremoving solvent until the preservation sample dries to form a highlyviscous liquid.

The process is very gentle and does not expose the active agent tofreezing or boiling and is therefore advantageous over conventionalfreeze drying and foam drying techniques which would subject the sampleto one or both of these stresses. Where the active agent to be preservedis labile, the use of the method of the invention leads to increasedretention of activity and/or antigenicity. This can be measured byreconstituting the dried active agent in solvent, preferably water or anaqueous solution, and measuring the activity or antigenicity by astandard assay (for example by ELISA) and comparing the results withthat obtained with either an undried sample or with samples dried byfreeze drying or foam drying techniques, and then reconstituted.

It is particularly advantageous to dry IPV (inactivated polio virus, theimmunogen in injectable polio vaccine) using the process of theinvention. IPV is present in known vaccines as a liquid formulation(WO99/48525). Problems have arisen on attempting to use a solidformulation of IPV in a vaccine since standard freeze drying procedureslead to a loss of IPV antigenicity. The process of the invention leadsto much higher retention of the polio virus antigens, due partially tothe reduced time required by the process of the invention.

The process of the invention is advantageous over normal freeze dryingsince the running cycle is shorter and requires less refrigerationmaking it more energy efficient. Since the drying process is often therate limiting step of a process, the use of the method of the inventionleads to higher levels of production at reduced expense.

DESCRIPTION OF FIGURES

FIG. 1—Photograph of the high viscosity liquid in inverted vials.

DETAILED DESCRIPTION

The method of the invention is used for preserving an active agent andcomprises the steps of:

-   -   a) preparing a preservation sample by suspending or dissolving        an active agent in a solution of a stabilizing agent;    -   b) subjecting the preservation sample to such temperature and        pressure conditions that the preservation sample looses solvent        by evaporation, without freezing or bubbling to form a foam, to        form a viscous liquid;        and optionally includes a further step of:    -   c) removing solvent until the viscous liquid dries to form a        highly viscous liquid.

A method of preserving an active agent produces a form of the activeagent that is able to withstand extended storage during which theactivity and/or antigenicity and/or immunogenicity of the active agentis maintained. Preferably the active agent retains at least 40, 50, 60,70, preferably 80, 90, 95% of its original activity, antigenicity and/orimmunogenicity over a period of at least 3, 6, 9, 12, 24 months storageat 4° C. Antigenicity or immunogenicity can be measured by standardassays as described below.

The method is particularly useful for extending the shelf life of labileproducts which rapidly loose activity when stored in solution or whenexposed to freezing or bubbling to form a foam.

A labile product is prone to loss of activity and/or to loss ofantigenicity and/or loss of immunogenicity, following storage insolution and/or freezing and/or subjecting to stresses such as thoseinvolved in bubbling during foam formation.

It is particularly applicable for use where a lower concentration (e.g.3%-15% w/v) of the glass forming polyol is advantageous and a shorterdrying process (less than 4, 6, 8, 10 or 12 hours) is preferred.

A viscous liquid is defined as the product of the primary phase ofsolvent removal, at the end of which the majority of solvent has beenlost from the sample. This point can be recognized because the rate ofevaporation slows down so that the temperature of the sample returns tothe ambient temperature as the endothermic effect of bulk evaporation islost.

A highly viscous liquid is produced after the viscous liquid produced atthe end of the primary phase of drying has been exposed to reducedpressure for a further period of time after the end of the primary phaseof drying. A highly viscous liquid has a solvent content less than orequal to 15, 12, 10, 8, 5, 4, 3, 2 or 1% (w/w), preferably as determinedby Karl Fischer coulometric moisture analyzer (Eur. J. Pharm. Biopharm.(2000) 50; 277-284). Preferred ranges of solvent content are 1-3%, 3-5%,5-10% or 10-15% (w/w). The highly viscous liquid has a sufficiently lowsolvent content such that the active agent is preserved in a stablestate for at least 3, 6, 9,12 or 24 months at 4° C., allowing the activeagent to retain at least 40, 50, 60, preferably 70, 80, 90, 95% of itsactivity and/or antigenicity and/or immunogenicity over this period.Preferably, the highly viscous liquid has a solid appearance but is arubber or glass, preferably a glass and is able to flow very slowly overa period of 2, 4, or 6 days, preferably 1, 2, 3 or 4 weeks, morepreferably 2, 4, 6, 8, 10 or 12 months. The extremely slow flow may bemeasured by inverting a receptacle containing the highly viscous liquidand leaving at room temperature until the highly viscous liquid isobserved to flow. In a preferred embodiment, the highly viscous liquidwill not appear to flow after 2, 4 or 6 days, preferably 1, 2, 3, or 4weeks, more preferably 2, 4, 6, 8, 10 or 12 months in an invertedposition. Preferably the highly viscous liquid has a clear, transparentappearance.

Preparation of the Preservation Sample

Any stabilizing agent is suitable for use in the first step of thisinvention. Suitable materials include, but are not limited to, allpolyols, including carbohydrate and non-carbohydrate polyols. Preferablythe stabilizing polyol enables the active agent to be stored withoutsubstantial loss of activity by denaturation, aggregation or othermeans. Particularly suitable materials include sugars, sugar alcoholsand carbohydrate derivatives. Preferably, the glass forming polyol is acarbohydrate or derivatives thereof, including glucose, maltulose,iso-maltulose, lactulose, sucrose, maltose, lactose, iso-maltose,maltitol, lactitol, palatinit, trehalose, raffinose, stachyose,melezitose or dextran, most preferably trehalose, sucrose, sorbitol,raffinose, mannitol, lactose, lactitol or palatinit, most preferablysucrose, sorbitol, lactose or trehalose.

Bacterial polysaccharides are particularly advantageous for use as astabilizing agent in an immunogenic composition since they can act bothas a stabilizing agent and an immunogen.

Carbohydrates include, but are not limited to, monosaccharides,disaccharides, trisaccharides, oligosaccharides and their correspondingsugar alcohols, polyhydroxyl compounds such as carbohydrate derivativesand chemically modified carbohydrates, hydroxyethyl starch and sugarcopolymers. Both natural and synthetic carbohydrates are suitable foruse. Synthetic carbohydrates include, but are not limited to, thosewhich have the glycosidic bond replaced by a thiol or carbon bond. BothD and L forms of the carbohydrates may be used. The carbohydrate may benon-reducing or reducing. Where a reducing carbohydrate is used, theaddition of inhibitors of the Maillard reaction is preferred.

Reducing carbohydrates suitable for use in the invention are those knownin the art and include, but are not limited to, glucose, maltose,lactose, fructose, galactoase, mannose, maltulose and lactulose.Non-reducing carbohydrates include, but are not limited to, non-reducingglycosides of polyhydroxyl compounds selected from sugar alcohols andother straight chain polyalcohols. Other useful carbohydrates includeraffinose, stachyose, melezitose, dextran, sucrose, cellibiose,mannobiose and sugar alcohols. The sugar alcohol glycosides arepreferably monoglycosides, in particular the compounds obtained byreduction of disaccharides such as lactose, maltose, lactulose andmaltulose.

Particularly preferred carbohydrates are trehalose, sucrose, sorbitol,maltitol, lactitol, palatinit and glucopyranosyl-1→6-mannitol.

Amino acids can act as stabilizing agents and can be used by themselvesand preferably in combination with a polyol. Preferred amino acidsinclude glycine, alanine, arginine, lysine and glutamine although anyamino acid, or a combination of amino acids, peptide, hydrolyzed proteinor protein such as serum albumin can act as a stabilizing agent.

The concentration of the stabilizing agent used in the process of theinvention may be between 1% and 50% weight/volume, preferably 1-5%,5-10%, 5-10%, 15-20%, 20-25% or 25-50%, most preferably less than orequal to 15% or 10% (w/v). The amounts of stabilizing agent required isproportional to the amount of salts present. Therefore, although levelsof stabilizing agent between 2% and 10% are preferred, higherconcentrations of 10% to 25% may be required to dry samples with a highsalt (over 100 mM, 200 mM, 300 mM, 400 mM or 500 mM) content.

Preferably, the preservation sample will contain a component capable ofinhibiting crystal formation in the highly viscous liquid of theinvention. Salts and other molecules including amino acids and phenolred inhibit crystal formation.

Container

Different mixtures and various container shapes and sizes can beprocessed simultaneously. Ideally, the container size used is sufficientto contain the initial mixture and accommodate the volume of the solidformed thereof. Typically, this is determined by the mass of the glassforming material, the surface area of the container and the conditionsof the glass formation. The mass of glass forming material must besufficient to give viscous syrup which translates practically as aminimal mass per unit area of container surface. This ratio varies frommixture to mixture and container used, but is easily determinedempirically by one skilled in the art by following the procedures setforth herein. Any such vials can be used, including Wheaton moulded andtube-cut vials.

The process of the invention preferably uses containers with a solventrepellent, preferably a water repellent interior surface. This isachieved through coating the interior surface with a hydrophobiccomposition, for instance by siliconization. Siliconization is achievedby processes that are well known to those skilled in the art. In onemethod, the container is siliconized by rinsing the interior of thecontainer with an emulsion of silicone, followed by processing throughan oven at high temperature, typically 350° C. Alternatively, the waterrepellent interior surface is achieved by the container being made of awater repellent composition.

The water repellent interior surface of the container makes the driedproduct of the process easier to reconstitute since less of the watercollects on the sides of the container.

Although singular forms may be used herein, more than one glassmatrix-forming material, more than one additive, and more than onesubstance may be present. Effective amounts of these components areeasily determined by one skilled in the art.

Solution

The solvent into which the stabilizing agent and active agent are mixedcan be aqueous, organic, or a mixture of both. Sufficient aqueoussolvent to dissolve the glass matrix-forming material and sufficientorganic solvent to dissolve a hydrophobic substance may be used,allowing the formation of glass incorporating hydrophobic substance(s).

The choice of solvent will depend upon the nature of the material chosenfor glass matrix formation, as well as the nature of any additive and/orsubstance to be incorporated. The solvent should be of a nature and ofsufficient volume to effect adequate solubilization of the glassmatrix-forming material as well as any additive and/or substance. If thesubstance is a hydrophilic material, the liquid will preferably beaqueous to avoid any potential loss of activity due to deleterioussolvent interactions. Preferably, the aqueous solvent includes anysuitable aqueous solvent known in the art, including, but not limitedto, water and biological buffer solutions. Preferably, the aqueoussolvent is present in an amount of 5 to 98% by volume, more preferably80-98% by volume, most preferably 85-98% by volume.

The volume of solvent can vary and will depend upon the glassmatrix-forming material and the substance to be incorporated as well asany additives. The minimum volume required is an amount necessary tosolubilize the various components. However, homogeneously dispersedsuspensions of the substance(s) can also be used. Suitable amounts ofthe components in specific embodiments are easily determinable by thoseskilled in the art in light of the examples provided herein.

Various additives can be introduced into the preservation sample. Apreferred additive is an inhibitor of the Maillard reaction. Preferably,if the substance and/or glass matrix-forming material contains carbonyland amino, imino or guanidino groups, the compositions further containat least one physiologically acceptable inhibitor of the Maillardreaction in an amount effective to substantially prevent condensation ofamino groups and reactive carbonyl groups in the composition. Theinhibitor of the Maillard reaction can be any known in the art. Theinhibitor is present in an amount sufficient to prevent, orsubstantially prevent, condensation of amino groups and reactivecarbonyl groups. Typically, the amino groups are present on thesubstance and the carbonyl groups are present on the glass matrixforming material, or the converse. However, the amino acids and carbonylgroups may be intramolecular within either the substance or thecarbohydrate.

Various classes of compounds are known to exhibit an inhibiting effecton the Maillard reaction and hence to be of use in the compositionsdescried herein. These compounds are generally either competitive ornon-competitive inhibitors of the Maillard reaction. Competitiveinhibitors include, but are not limited to, amino acid residues (both Dand L), combinations of amino acid residues and peptides. Particularlypreferred are lysine, arginine, histidine and tryptophan. Lysine andarginine are the most effective. There are many known non-competitiveinhibitors. These include, but are not limited to, aminoguanidine andderivatives and amphotericin B. EP-A-0 433 679 also describes suitableMaillard inhibitors which include 4-hydroxy-5,8-dioxoquinolinederivatives.

It is advantageous to incorporate a colored dye into the preservationsample in order to allow easier visualization of the dried product ofthe method of the invention. This is particularly important duringreconstitution to ensure that the highly viscous liquid is thoroughlyreconstituted prior to use. Preferably, the colored dye maintains itscolor at a neutral pH and is compatible with injection into a patient.Most preferably the colored dye is phenol red.

Loss of Solvent by Evaporation (Evaporative Drying—Step b)

The process of the invention involves subjecting the preservation sampleto such pressure and temperature conditions so that the preservationsample looses solvent by evaporation, without the sample freezing orbubbling to form a foam.

The temperature within the preservation sample will, at times, bedifferent from that external to the sample due to the endothermic natureof the evaporation process. References to temperature are to theconditions external to the preservation sample, for instance, where alarge industrial freeze dryer is used, to the temperature of the shelfThis usually corresponds to the freeze dryer temperature setting.

Optionally a preliminary step of degassing the preservation sample ispresent in the method of the invention. The pressure is reduced to at orbelow 200 mBars, preferably between 200 and 35 mBars, for a period of atleast 5 minutes before the pressure is reduced further.

A preferred embodiment of the invention achieves evaporative drying byreducing the pressure while controlling the temperature conditions. Thepressure is adjusted to at or below 30, 25, 20, preferably 15, 12, mostpreferably 10, 8, 7, 6, 5, 4, 3, 2 or 1 mbar, while maintaining thetemperature setting at a temperature above 0° C., preferably of between5° C. to 37° C., 4° C. to 10° C., 10° C. to 15° C.; 15° C. to 20° C.;20° C. to 25° C.; 25° C. to 30° C.; 30° C. to 37° C. or 37° C. to 45° C.. These conditions are maintained for at least 1, 2, 3, 4, 5, 8, 10, 12,16 or 24 hours, preferably for between 2-4 hours, 4-6 hours, 6-8 hours,8-12 hours or 12-18 hours. In a particularly preferred embodiment, thepressure is maintained above 2 mbars where the temperature setting is15° C. in order to prevent freezing of the sample. In a preferredembodiment, the temperature is maintained at 15° C. and the pressure isset to between 5-10 mBars, more preferably 6-9 mBars, most preferablyaround 8 mBars. Where a higher temperature setting is used, slightlylower pressure is possible without freezing the sample and where a lowertemperature setting is used, the pressure should be maintained at thehigher level to prevent freezing. Preferably the conditions aremaintained for a sufficient period of time so that the evaporation ratehas slowed so that the temperature of the sample is approximately thesame as that external to the sample.

Preferably, the preservation sample does not freeze or bubble/boil toform a foam and looses solvent to form a viscous liquid or a highlyviscous liquid.

Removing Solvent to Form a Highly Viscous Liquid

A subsequent stage of the method of the invention involves removingsolvent until the preservation sample dries to form a highly viscousliquid. The sample neither freezes nor bubbles to form a foam during thesecondary drying phase.

A highly viscous liquid is defined as a material with a solvent contentless than or equal to 15, 12, 10, more preferably 8, 5, 4, 3, 2 or 1%(w/w) preferably measure using a Karl Fischer coulometric moistureanalyzer. The highly viscous liquid has a sufficiently low solventcontent such that the active agent is preserved in a stable state for atleast 3, 6, 9, 12 or 24 months at 4° C., allowing the active agent toretain at least 40, 50, 60, preferably 70, 80, 90, 95% of its activityand/or antigenicity and/or immunogenicity over this period. Preferably,the highly viscous liquid has a solid, and/or clear appearance but is aglass and is able to flow very slowly over a period of 2, 4, or 6 days,preferably 2, 3 or 4 weeks, more preferably 2, 4, 6, 8, 10 or 12 months.The extremely slow flow may be measured by inverting a receptaclecontaining the highly viscous liquid and leaving at room temperatureuntil the highly viscous liquid is observed to flow. In a preferredembodiment, the highly viscous liquid will not appear to flow after 2, 4or 6 days, preferably 2, 3 or 4 weeks, more preferably 2, 4, 6, 8, 10 or12 months in an inverted position.

In one embodiment of the invention, this is achieved by maintaining thepressure and temperature conditions at those applied in the firstevaporative drying stage. For instance, the pressure is maintained at orbelow at or below 30, 25, 20, preferably 15, 12, most preferably 10, 8,7, 6, 5, 4, 3, 2 or 1 mbar, while maintaining the temperature setting ata temperature above 0° C., preferably of between 5° C. to 37° C., 5° C.to 10° C., 10° C. to 15° C.; 15° C. to 20° C.; 20° C. to 25° C.; 25° C.to 30° C.; or 30° C. to 37° C. For a temperature setting of 15° C., apressure of 5-10 mBars, preferably 6-9 mBars, most preferably around 8mBars is maintained for between 4-24 hours, preferably 1-4 , 4-8, 8-12or 12-16 hours. These temperature and pressure conditions are maintainedfor 1, 2, 3, 4, 5, 6, 8, 10, 12, 18 hours or more in order to obtain ahighly viscous liquid with a solvent content less than or equal to 15,12, preferably 10, 8, 5, 4, 3, 2 or 1% (w/w) preferably measured by aKarl Fischer coulometric moisture analyzer.

Another embodiment of the invention increases the temperature settingduring solvent removal to a higher temperature setting than thatmaintained earlier in the process. This allows the solvent to leave thesample at a quicker rate so that the method of the invention can becompleted in a shorter time. For instance, the temperature setting isincreased to above 0° C., more preferably above 20° C., preferablybetween 5° C. and 37° C., 5° C. and 10° C., 10° C. and 20° C.; 20° C.and 30° C.; more preferably 30° C. and 40° C.; more preferably 40° C.and 50° C.; most preferably 50° C. and 60° C. while maintaining thepressure at or below 30, 25, 20, preferably 15, 12, most preferably 10,8, 7, 6, 5, 4, 3, 2 or 1 mbar. These temperature and pressure conditionsare maintained for at least 1, 2, 3, 4, 5, 6, 8, 10, 12 or 18 hours ormore in order to obtain a solid with solvent content less than or equalto 15, 12, 10, 8, 5, 4, 3, 2 or 1% (w/w) preferably measured by a KarlFischer coulometric moisture analyzer. This embodiment requires theactive agent to be heat stable at the temperature used for the method tobe carried out successfully.

A preferred embodiment of the invention reduces the pressure settingduring solvent removal (step c) to a lower pressure setting than thatused earlier in the process (step b). This allows the solvent to leavethe sample at a quicker rate so that the method of the invention can becompleted in a shorter time. It also enables a higher proportion of thesolvent to be lost. For instance, the pressure setting is set to at orbelow 7, 6, preferably 5, 4, 3, more preferably 2, 1.5, 1, mostpreferably 0.8, 0.5, 0.2, 0.1, 0.05, 0.02, 0.01, or 0.005 mbar, whilemaintaining the temperature at or above 0° C., preferably between 10° C.and 20° C.; 20° C. and 30° C.; 30° C. and 35° C. or above 40° C. Thesetemperature and pressure conditions are maintained for 1, 2, 3, 4, 5, 6,8, 10, 12 or 18 hours or more in order to obtain a solid with a solventcontent less than or equal to 15, 12, preferably 10, 8, 5, 4, 3, 2 or 1%(w/w) preferably as determined by Karl Fischer coulometric moistureanalyser (Eur. J. Pharm. Biopharm. (2000) 50; 277-284).

Preferably, steps b) and c) (or b) alone) should be completed in a timeequal to or less than 18 hours, preferably 16, 12, 10 hours, mostpreferably 8, 6, 5 or 4 hours.

Active Agent

The method of the invention is useful for preserving any active agenthowever it is particularly useful in the case of labile active agentsthat loose activity and/or antigenicity and/or immunogenicity duringother preservation processes.

The active agent to be preserved using a method of the invention maycomprise a biological system selected from the group consisting ofcells, subcellular compositions, bacteria, outer membrane vesiclepreparations and viruses, virus components or virus like particles. Itmay also comprise molecules, for instance proteins, peptides, aminoacids, polynucleic acids, oligonucleotides, polysaccharides,oligosaccharides, polysaccharide—protein conjugates,oligosaccharide-protein conjugates.

Examples of active agents that can be preserved using a method of theinvention include any bioactive substances such as pharmaceuticallyeffective substances, including, but not limited to, antiinflammatorydrugs, analgesics, tranquillizers, antianxiety drugs, antispasmodics,antidepressants, antipsychotics, tranquillizers, antianxiety drugs,narcotic antagonists, antiparkinsonism agents, cholinergic agonists,chemotherapeutic drugs, immunosuppressive agents, antiviral agents,antimicrobial agents, appetite suppressants, anticholinergics,antimetrics, antihistaminics, antimigraine agents, coronary, cerebal orperipheral vasodilators, hormonal agents, contraceptives, antithromboticagents, diueretics, antihypertensive agents, cardiovascular drugs,oploids, and the like.

Suitable agents also include therapeutic and prophylactic agents. Theseinclude, but are not limited to, any therapeutically effectivebiological modifier. Such substances include, but are not limited to,subcellular compositions, cells, bacteria, outer membrane vesiclepreparations, viruses and molecules including but not limited to,lipids, organics, proteins and peptides (synthetic and natural), peptidemimetics, hormones (peptide, steroid and corticosteroid), D and L aminoacid polymers, oligosaccharides, polysaccharides, nucleotides,oligonucleotides and nucleic acids, including DNA and RNA, proteinnucleic acid hybrids, small molecules and physiologically activeanalogues thereof. Further, the modifiers may be derived from naturalsources or made by recombinant or synthetic means and include analogues,agonists and homologs.

As used herein “protein” refers also to peptides and polypeptides. Suchproteins include, but are not limited to, enzymes, biopharmaceuticals,growth hormones, growth factors, insulin, antibodies, both monoclonaland polyclonal and fragments thereof, interferons, interleukins andcytokines.

Therapeutic nucleic acid-based agents prepared by the methods describedherein are also encompassed by the invention. As used herein, “nucleicacids” includes any therapeutically effective nucleic acids known in theart including, but not limited to DNA, RNA, and physiologically activeanalogues thereof. The nucleotides may encode genes or may be any vectorknown in the art of recombinant DNA including, but not limited to,plasmids, retroviruses and adeno-associated viruses.

The preservation of substances which are prophylactically active andcarriers thereof are further encompassed by the invention. Preferablecompositions include immunogens such as vaccines. Vaccines may be fororal administration or may be for injection after reconstitution.Suitable vaccines include, but are not limited to, live and attenuatedviruses, nucleotide vectors encoding antigens, live and attenuatedbacteria, protein, polysaccharide, oligosaccharide and/orlipopolysaccharide antigens, antigens plus adjuvants and antigens and/orhaptens coupled to carriers. Particularly preferred are vaccineseffective against diptheria, tetanus, pertussis, botulinum, cholera,Dengue, Hepatitis A, B, C and E, Haemophilus influenzae b, Streptococcuspneumoniae, Neisseria meningitidis, Neisseria gonorrhoeae,Staphylococcus aureus, Staphylococcus epidermidis, Group B streptococci,Group A streptococci, herpes virus, Helicobacterium pylori, influenza,Japanese encephalitis, meningococci A, B, C, Y, W, measles, mumps,papilloma virus, pneumococci, polio virus, inactivated polio virus(IPV—preferably comprising types 1, 2 and 3 as is standard in thevaccine art, most preferably the Salk polio vaccine), rubella,rotavirus, respiratory syncytial virus, Shigella, tuberculosis,varicella-zoster virus, yellow fever and combinations thereof. Theantigenic component of vaccines may also be produced by molecularbiology techniques to produce recombinant peptides or fusion proteinscontaining one or more portions of a protein derived from a pathogen.For instance, fusion proteins containing an antigen and the B subunit ofcholera toxin have been shown to induce an immune response to theantigen. Sanches et al (1989) Proc. Natl. Acad. Sci. USA 86:481-485.Vaccines are particularly suitable for incorporation into thesingle-dosage composition. They are stable indefinitely under ambientconditions and can be redissolved in sterile diluent immediately beforeinoculation.

In a preferred embodiment, the immunogenic composition would comprisecapsular polysaccharides derived from one or more of serogroups A, C,W-135 and Y of Neisseria meningitidis. A further preferred embodimentwould comprise capsular polysaccharides derived from Streptococcuspneumoniae. The pneumococcal capsular polysaccharide antigens arepreferably selected from serotypes 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V,10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F and 33F (mostpreferably from serotypes 1, 3, 4, 5, 6B, 7F, 9V, 14, 18C, 19F and 23F).A further preferred embodiment would contain the PRP capsularpolysaccharides of Haemophilus influenzae type b. A further preferredembodiment would contain the Type 5, Type 8, 336 or PNAG capsularpolysaccharides of Staphylococcus aureus. A further preferred embodimentwould contain the Type I, Type II, Type III or PIA capsularpolysaccharides of Staphylococcus epidermidis. A further preferredembodiment would contain the Type Ia, Type Ic, Type II or Type IIIcapsular polysaccharides of Group B streptocoocus. A further preferredembodiment would contain the capsular polysaccharides of Group Astreptococcus, preferably further comprising at least one M protein andmore preferably multiple types of M protein.

In one embodiment of the invention, the bacterial polysaccharides arefull length, being purified native polysaccharides. In an alternativeembodiment of the invention, the polysaccharides are sized between 2 and20 times, preferably 2-5 times, 5-10 times, 10-15 times or 15-20 times,so that the polysaccharides are smaller in size for greatermanageability. Oligosaccharides are used in a preferred embodiment.Oligosaccharides typically contain between 2 and 20 repeat units.

Polysaccharide and oligosaccharides may be unconjugated or conjugated asdescribed below.

Combinations of two or more of the above active agents may be preservedusing the method of preservation of the invention. Part or all of avaccine may be preserved using the method of preservation of theinvention.

A preferred active agent to be preserved using the process of theinvention comprises IPV (an inactivated mixture of polio virus strains).IPV, particularly the type 3 component, is sensitive to conventionalfreeze drying and foam drying techniques as shown by the loss ofantigens following freeze drying or foam drying and subsequentreconstitution.

IPV is defined as inactivated polio virus (preferably comprising types1, 2 and 3 as is standard in the vaccine art, most preferably the Salkpolio vaccine). A vaccine dose of IPV contains 20-80, preferably 40 or80 D-antigen units of type 1 (Mahoney), 4-16, preferably 8 or 16D-antigen units of type 2 (MEF-1) and 20-64, preferably 32 or 64D-antigen units of type 3 (Saukett).

When dried by a method of the invention, preferably the antigenicity of1, 2, or all 3 of types 1, 2 and 3 of polio virus are retained; morepreferably the antigenicity of type 1; type 2; type 3; type 1 and type2; type 1 and type 3; type 2 and type 3; or type 1, type 2 and type 3 isretained at a level of at least 40%, 50%, 60%, 70%, 80%, 90%, 95% or 98%of the antigenicity of a reference sample which has not been subjectedto the drying process. This can be measured, following reconstitution ofthe highly viscous liquid in an aqueous solution, by any suitable methodincluding by ELISA using polyclonal and/or monoclonal antibodies againstpolio virus type 1, 2 and/or 3.

When dried by a method of the invention, preferably the immunogenicityof 1, 2, or all 3 of types 1, 2 and 3 of polio virus are retained; morepreferably the immunogenicity of type 1; type 2; type 3; type 1 and type2; type 1 and type 3; type 2 and type 3; or type 1, type 2 and type 3 isretained at a level of at least 40%, 50%, 60%, 70%, 80%, 90%, 95% or 98%of the immunogencity of a reference sample which has not been subjectedto the drying process. This can be measured, following reconstitution ofthe highly viscous liquid in an aqueous solution, by any suitablemethod. In a preferred method, the highly viscous liquid isreconstituted in an aqueous solution and is inoculated into an animal,preferably a rat. After a suitable period of time, antisera arecollected from the inoculated animals and seroconversion is tested.Preferably, a relative potency of at least 0.4, 0.5, 0.6, 0.7, 0.8 or0.9 is achieved, compared to an undried reference sample.

Preferably, IPV is combined with one or more of Hib (Haemophilusinfluenzae type b) PRP polysaccharide or oligosacchairde and/ormeningococcal A, C, W and/or Y polysaccharides or oligosaccharide and/orpneumococcal polysaccharides or oligosaccharide. Most preferably theactive agents comprise, IPV and Hib; IPV and MenC; IPV, Hib and MenC;Hib and MenC; IPV and MenA and C; Hib and Men A and C; IPV, Hib, Men Aand C; Hib, Men C and Y; or IPV, Hib, Men C and Y.

The above particularized active agents may also comprise one or morepneumococcal capsular polysaccharides as described below.

In the above compositions where polysaccharides are used,oligosaccharides may also be employed (as defined below).

Although these compositions may be adjuvanted (as described below), theyare preferably unadjuvanted or preferably do not comprise aluminiumsalts.

Preferably the polysaccharides or oligosaccharides are conjugated to apeptide or carrier protein comprising T-helper epitopes (as describedbelow).

Additional Components

The preferred combinations, dried by the process of the invention may becombined with other antigens in a combination vaccine which isdesiccated or is preferably a liquid formulation which can be used toreconstitute the dried components. Preferred antigens to be combinedwith the active agents in the paragraph above include one or more ofdiphtheria toxoid, tetanus toxoid, whole cell pertussis (Pw), acellularpertussis (Pa) (as described below), Hepatitis B surface antigen,Hepatitis A virus, Haemophilus influenzae b polysaccharides, neisserialpolysaccharides, N. meningitidis serotype B proteins, pneumococcalpolysaccharides, pneumococcal proteins or any of the antigens listedbelow. Bacterial polysaccharides may be conjugated to a carrier proteinsuch as tetanus toxoid, tetanus toxoid fragment C, diphtheria toxoid,CRM197, pneumolysin, Protein D (U.S. Pat. No. 6,342,224) as describedbelow.

Active agents preserved using the process of the invention may beformulated with capsular polysaccharides derived from one or more ofNeisseria meningitidis, Haemophilus influenzae b, Streptococcuspneumoniae, Group A Streptococci, Group B Streptococci, Staphylococcusaureus or Staphylococcus epidermidis. In a preferred embodiment, theimmunogenic composition would comprise capsular polysaccharides derivedfrom one or more of serogroups A, C, W-135 and Y of Neisseriameningitidis. A further preferred embodiment would comprise capsularpolysaccharides derived from Streptococcus pneumoniae. The pneumococcalcapsular polysaccharide antigens are preferably selected from serotypes1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A,19F, 20, 22F, 23F and 33F (most preferably from serotypes 1, 3, 4, 5,6B, 7F, 9V, 14, 18C, 19F and 23F). A further preferred embodiment wouldcontain the PRP capsular polysaccharides of Haemophilus influenzae typeb. A further preferred embodiment would contain the Type 5, Type 8, 336or PNAG capsular polysaccharides of Staphylococcus aureus. A furtherpreferred embodiment would contain the Type I, Type II, Type III or PIAcapsular polysaccharides of Staphylococcus epidermidis. A furtherpreferred embodiment would contain the Type Ia, Type Ic, Type II or TypeIII capsular polysaccharides of Group B streptocoocus. A furtherpreferred embodiment would contain the capsular polysaccharides of GroupA streptococcus, preferably further comprising at least one M proteinand more preferably multiple types of M protein.

In one embodiment of the invention, the bacterial polysaccharides arefull length, being purified native polysaccharides. In an alternativeembodiment of the invention, the polysaccharides are sized between 2 and20 times, preferably 2-5 times, 5-10 times, 10-15 times or 15-20 times,so that the polysaccharides are smaller in size for greatermanageability. Oligosaccharides are used in a preferred embodiment.Oligosaccharides typically contain between 2 and 20 repeat units.

Such capsular polysaccharides may be unconjugated or conjugated to acarrier protein such as tetanus toxoid, tetanus toxoid fragment C,diphtheria toxoid, CRM197, pneumolysin, Protein D (U.S. Pat. No.6,342,224). Tetanus toxin, diphtheria toxin and pneumolysin aredetoxified either by genetic mutation and/or preferably by chemicaltreatment.

The polysaccharide conjugate may be prepared by any known couplingtechnique. For example the polysaccharide can be coupled via a thioetherlinkage. This conjugation method relies on activation of thepolysaccharide with 1-cyano-4-dimethylamino pyridinium tetrafluoroborate(CDAP) to form a cyanate ester. The activated polysaccharide may thus becoupled directly or via a spacer group to an amino group on the carrierprotein. Preferably, the cyanate ester is coupled with hexane diamineand the amino-derivatized polysaccharide is conjugated to the carrierprotein using heteroligation chemistry involving the formation of thethioether linkage. Such conjugates are described in PCT publishedapplication WO93/15760 Uniformed Services University.

The conjugates can also be prepared by direct reductive aminationmethods as described in U.S. Pat. No. 4,365,170 (Jennings) and U.S. Pat.No. 4,673,574 (Anderson). Other methods are described in EP-0-161-188,EP-208375 and EP-0-477508.

A further method involves the coupling of a cyanogen bromide activatedpolysaccharide derivatized with adipic acid hydrazide (ADH) to theprotein carrier by Carbodiimide condensation (Chu C. et al Infect.Immunity, 1983 245 256).

Preferred pneumococcal proteins antigens are those pneumococcal proteinswhich are exposed on the outer surface of the pneumococcus (capable ofbeing recognised by a host's immune system during at least part of thelife cycle of the pneumococcus), or are proteins which are secreted orreleased by the pneumococcus. Most preferably, the protein is a toxin,adhesin, 2-component signal tranducer, or lipoprotein of Streptococcuspneumoniae, or fragments thereof. Particularly preferred proteinsinclude, but are not limited to: pneumolysin (preferably detoxified bychemical treatment or mutation) [Mitchell et al. Nucleic Acids Res. 1990Jul. 11; 18(13): 4010 “Comparison of pneumolysin genes and proteins fromStreptococcus pneumoniae types 1 and 2.”, Mitchell et al. BiochimBiophys Acta 1989 Jan. 23; 1007(1): 67-72 “Expression of the pneumolysingene in Escherichia coli: rapid purification and biologicalproperties.”, WO 96/05859 (A. Cyanamid), WO 90/06951 (Paton et al), WO99/03884 (NAVA)]; PspA and transmembrane deletion variants thereof (U.S.Pat. No. 5,804,193—Briles et al.); PspC and transmembrane deletionvariants thereof (WO 97/09994—Briles et al); PsaA and transmembranedeletion variants thereof (Berry & Paton, Infect Immun 1996December;64(12):5255-62 “Sequence heterogeneity of PsaA, a 37-kilodaltonputative adhesin essential for virulence of Streptococcus pneumoniae”);pneumococcal choline binding proteins and transmembrane deletionvariants thereof; CbpA and transmembrane deletion variants thereof (WO97/41151; WO 99/51266); Glyceraldehyde-3-phosphate—dehydrogenase(Infect. Immun. 1996 64:3544); HSP70 (WO 96/40928); PcpA (Sanchez-Beatoet al. FEMS Microbiol Lett 1998, 164:207-14); M like protein, (EP0837130) and adhesin 18627, (EP 0834568). Further preferred pneumococcalprotein antigens are those disclosed in WO 98/18931, particularly thoseselected in WO 98/18930 and PCT/US99/30390.

Preferred Neisserial proteins to be formulated with the immunogeniccomposition of the invention include ThpA (WO93/06861; EP586266;WO092/03467; U.S. Pat. No. 5,912,336), TbpB (WO93/06861; EP586266), Hsf(WO99/31132), NspA (WO96/29412), Hap (PCT/EP99/02766), PorA, PorB, OMP85(also known as D15) (WO00/23595), PilQ (PCT/EP99/03603), PldA(PCT/EP99/06718), FrpB (WO96/31618 see SEQ ID NO:38), FrpA or FrpC or aconserved portion in common to both of at least 30, 50, 100, 500, 750amino acids (WO92/01460), LbpA and/or LbpB (PCT/EP98/05117; Schryvers etal Med. Microbiol. 1999 32: 1117), FhaB (WO98/02547), HasR(PCT/EP99/05989), lipo02 (PCT/EP99/08315), MltA (WO99/57280) and ctrA(PCT/EP00/00135). Neisserial proteins are preferably added as purifiedproteins of as part of an outer membrane preparation.

The vaccine is preferably formulated with antigens providing protectionagainst one or more of Diphtheria, Tetanus and Bordetella pertussisinfections. The pertussis component may be killed whole cell B.pertussis (Pw) or acellular pertussis (Pa) which contains at least oneantigen (preferably two or all three) from PT, FHA and 69kDa pertactin.Certain other acellular vaccines also contain agglutinogens such as Fim2and Fim 3 and these vaccines are also contemplated for use in theinvention. Typically, the antigens providing protection againstDiphtheria and Tetanus are Diphtheria toxoid and tetanus toxoid. Thetoxoids are chemically inactivated toxins (for example, followingtreatment with formaldehyde) or toxins inactivated by the introductionof one or more point mutations.

Alternatively the highly viscous liquid of the invention may be providedas a kit with the highly viscous liquid glass in one container andliquid DTPa or DTPw in another container. Such kits can for examplecomprise a dual chamber syringe with the dried and liquid componentscontained in the same syringe but in different chambers. The driedcomponent is then reconstituted with the liquid vaccine immediatelyprior to injection as a single vaccine. Thus for example, the highlyviscous liquid composition of the invention is reconstituted with theliquid DTPa or DTPw vaccine (preferably extemporaneously) andadministered as a single vaccine. The DTPa or DTPw vaccine typically isadjuvanted at least in part with aluminium hydroxide (for instanceInfanrix® and Tritanrix® vaccines of GlaxoSmithKline Biologicals s.a.).

The vaccine may also optionally comprise one or more antigens that canprotect a host against non-typeable Haemophilus influenzae, RSV and/orone or more antigens that can protect a host against influenza virus.

Preferred non-typeable H. influenzae protein antigens include Fimbrinprotein (U.S. Pat. No. 5,766,608) and fusions comprising peptidestherefrom (eg LB1 Fusion) (U.S. Pat. No. 5,843,464—Ohio State ResearchFoundation), OMP26, P6, protein D, ThpA, TbpB, Hia, Hmw1, Hmw2, Hap, andD15.

Preferred influenza virus antigens include whole, live or inactivatedvirus, split influenza virus, grown in eggs or MDCK cells, or Vero cellsor whole flu virosomes (as described by R. Gluck, Vaccine, 1992, 10,915-920) or purified or recombinant proteins thereof, such as HA, NP,NA, or M proteins, or combinations thereof.

Preferred RSV (Respiratory Syncytial Virus) antigens include the Fglycoprotein, the G glycoprotein, the HN protein, the M protein orderivatives thereof. It should be appreciated that antigeniccompositions of the invention may comprise one or more capsularpolysaccharide from a single species of bacteria. Antigenic compositionsmay also comprise capsular polysaccharides derived from one or morespecies of bacteria

Immunogenic Compositions and Vaccines

A further aspect of the invention includes immunogenic compositions orvaccines comprising the highly viscous liquid of the invention and apharmaceutically acceptable excipient.

Preferably, the immunogenic composition or vaccine contains an amount ofan adjuvant sufficient to enhance the immune response to the immunogen.Suitable adjuvants include, but are not limited to, aluminium salts,squalene mixtures (SAF-1), muramyl peptide, saponin derivatives,mycobacterium cell wall preparations, monophosphoryl lipid A, mycolicacid derivatives, non-ionic block copolymer surfactants, Quil A, choleratoxin B subunit, polphosphazene and derivatives, and immunostimulatingcomplexes (ISCOMs) such as those described by Takahashi et al. (1990)Nature 344:873-875. For veterinary use and for production of antibodiesin animals, mitogenic components of Freund's adjuvant can be used.

As with all immunogenic compositions or vaccines, the immunologicallyeffective amounts of the immunogens must be determined empirically.Factors to be considered include the immunogenicity, whether or not theimmunogen will be complexed with or covalently attached to an adjuvantor carrier protein or other carrier, route of administrations and thenumber of immunising dosages to be administered. Such factors are knownin the vaccine art and it is well within the skill of immunologists tomake such determinations without undue experimentation.

The active agent can be present in varying concentrations in the highlyviscous liquid or vaccine of the invention. Typically, the minimumconcentration of the substance is an amount necessary to achieve itsintended use, while the maximum concentration is the maximum amount thatwill remain in solution or homogeneously suspended within the initialmixture. For instance, the minimum amount of a therapeutic agent ispreferably one which will provide a single therapeutically effectivedosage. For bioactive substances, the minimum concentration is an amountnecessary for bioactivity upon reconstitution and the maximumconcentration is at the point at which a homogeneous suspension cannotbe maintained. In the case of single-dosed units, the amount is that ofa single therapeutic application. Generally, it is expected that eachdose will comprise 1-100 ug of protein antigen, preferably 5-50 ug andmost preferably 5-25 ug. Preferred doses of bacterial polysaccharidesare 10-20 ug, 10-5 ug, 5-2.5 ug or 2.5-1 ug. The preferred amount of thesubstance varies from substance to substance but is easily determinableby one of skill in the art.

Highly Viscous Liquid Comprising an Active Agent

Another aspect of the invention is a highly viscous liquid comprising anactive agent which is preferably obtainable or obtained using a methodof the invention. The active agent preferably retains its activityand/or antigenicity and/or immunogenicity following drying using themethod of the invention and subsequent reconstitution. Preferably atleast 40, 50, 60, 70, 80, 90, or 95% of the active agent's activity,antigenicity or immunogenicity is retained. This may be determined byany suitable method, for instance as described above.

Highly viscous liquids of the invention preferably comprise a glassforming polyol selected from the group consisting of gluscose,maltulose, iso-maltulose, lactulose, sucrose, maltose, lactose,sorbitol, iso-maltose, maltitol, lactitol, palatinit, trehalose,raffinose, stachyose, melezitose and dextran.

Highly viscous liquid of the invention may contain any of the activeagents described above. The active agent preserved by the highly viscousliquid may comprise a biological system, for instance cells, subcellularcompositions, bacteria, outer membrane vesicle preparations and viruses.It may alternatively or further comprise molecules, for exampleproteins, peptides, amino acids, polynucleic acids, oligonucleotides,polysaccharides, oligosaccharides, polysaccharide—protein conjugates,oligosaccharide-protein conjugates. It may also comprise combinations oftwo or more of the above active agents.

Preferred embodiments include a highly viscous liquid preferablyobtained or obtainable by a method of the invention wherein the activeagent is or comprises a vaccine or vaccine component. Preferredcomponents of the vaccine are described above and include IPV, morepreferably IPV and bacterial polysaccharides, preferably polysaccharidesor oligosaccharides from Haemophilus influenzae b and Neisseriameningitidis A, C, W and Y.

Preferred vaccine components include IPV (an inactivated mixture ofpolio virus strains). Preferably, IPV is combined with one or more ofHib PRP polysaccharide and/or meningococcal A, C, W and/or Ypolysaccharides and/or pneumococcal polysaccharides (as describedabove), more preferably IPV and Hib; IPV and MenC; IPV, Hib and MenC;Hib and MenC; IPV and MenA and C; Hib and Men A and C; IPV, Hib, Men Aand C; Hib, Men C and Y; or IPV, Hib, Men C and Y.

In the above compositions where polysaccharides are used,oligosaccharides may also be employed (as defined above).

Although these compositions may be adjuvanted (as described above), theyare preferably unadjuvanted or preferably do not comprise aluminiumsalts.

Preferably the polysaccharides or oligosaccharides are conjugated to apeptide or carrier protein comprising T-helper epitopes (as describedabove).

The highly viscous liquid of the invention are preferably combined withother antigens in a combination vaccine which are optionally desiccatedor preferably liquid formulations which can be used to reconstitute thedried components. Preferred antigens to be combined with the contents ofthe container of the invention include one or more of diphtheria toxoid,tetanus toxoid, whole cell pertussis (Pw), acellular pertussis (Pa) (asdescribed above), Hepatitis B surface antigen, pneumococcalpolysaccharides, pneumococcal proteins, neisserial polysaccharides,neisserial proteins. Bacterial polysaccharides may be conjugated to acarrier protein such as tetanus toxoid, tetanus toxoid fragment C,diphtheria toxoid, CRM197, pneumolysin, Protein D (U.S. Pat. No.6,342,224) as described above.

A further aspect of the invention is a method of making a vaccinecomprising the step of reconstituting the highly viscous liquid in anaqueous solution. In a preferred embodiment, the aqueous solutioncomprises Diphtheria toxoid, Tetanus toxoid and Pertussis (acellular orwhole cell) antigens and optionally further comprises hepatitis Bsurface antigen. The DTP vaccine is optionally at least in partadjuvanted with an aluminium salt, preferably aluminium hydroxide oraluminium phosphate.

Another embodiment of the invention is a kit comprising the highlyviscous liquid of the invention held in a first container and a vaccinecomprising liquid DTP (acellular or whole cell) in a second container. Adual chamber syringe may be used as described above.

All references or patent applications cited within this patentspecification are incorporated by reference herein.

EXAMPLES

The examples below are carried out using standard techniques, which arewell known and routine to those of skill in the art, except whereotherwise described in detail. The examples are illustrative, but do notlimit the invention.

Example 1 Establishment of Freezing Conditions

Samples were made by dissolving sucrose in water to give 1%, 5%, 10% and20% solutions. Samples were put into a Heto Drywinner 8-85 freeze dryerin which shelf temperature may be regulated to within 1° C., the finaltemperature of the condenser is −85° C., pressure is regulated with ableed valve and 6 thermocouples are available to measure the producttemperature. The shelf temperature setting was maintained at 15° C.throughout the process. The pressure was initially reduced to 200 mBarand maintained at this level for 10 minutes before reducing the pressurefurther to 50 mBars, 5 mBars, 2.5 mBars, 0.75 mBars, 0.4 mBars and 0.2mBars. Each pressure level was maintained for 20 minutes to allow thetemperature to equilibrate and the temperature of the sample was readusing a thermocouple. Thermocouples were attached to samples withdifferent sucrose concentrations and the temperatures recorded in table1 are mean values of the temperatures.

Results

All samples froze between 1.66 and 1.11 mbars, irrespective of theconcentration of sucrose present. The temperatures measured at differentpressures were very close to those predicted from the triple pointcurve. Therefore the presence of sucrose does not have a large effect onthe temperature of the samples at different pressures.

In order to avoid freezing of the sample, the pressure should bemaintained above 2 mBars for a shelf temperature of 15° C. At lowertemperatures the pressure should be maintained at a higher level whereasuse of a higher temperature would allow the pressure to be reducedfurther without the samples freezing.

TABLE 1 Measured Theoretical Pressure temperature temperatureLiquid/frozen 1000 mBar  15° C. liquid 50 mBar  15° C. liquid 5 mBar  1°C.  1° C. liquid 2.5 mBar  −5° C.  −7° C. liquid 0.75 mBar −21° C. −21°C. frozen 0.4 mBar −22° C. −27° C. frozen 0.2 mBar −27° C. −32° C.frozen

Example 2 Method for Drying without Freezing or Foam Formation

Preservation samples containing 5%, 10%, 15% and 25% sucrose were madeand added to vials. Samples were put into a freeze dryer at atemperature setting of 1520 C. throughout the process. The pressure wasinitially reduced to 200 mBars and maintained at this level for 10minutes to allow degassing before reducing the pressure further. Thepressure was further reduced to 8 mbars for two to three hours duringwhich time thermocouples inside the samples showed that the sampletemperature reduced to 4° C. due to evaporative cooling. After 2-3hours, the temperature of the samples returned to 15° C., indicatingthat evaporation under these temperature and pressure conditions wasnear completion. During this stage of the process, the sample did notboil to form a foam or freeze so that an active agent within the sampleis exposed to as little stress as possible. The sample has theappearance of viscous liquid.

Further drying of the samples was achieved by reducing the pressurefurther to 0.1 mbars while keeping the shelf temperature setting at 15°C. These conditions were maintained for a further 10-16 hours. Duringthis phase, the sample temperature remained at 15° C. since the rate ofevaporation was slow. Further drying took place and the resultant samplehad a solid appearance. If the sample was placed on its side, the samplecontents slowed very slowly, over a period of days showing that thesample is a liquid glass of high viscosity. FIG. 1 shows the appearanceof the high viscosity liquid.

Example 3 Retention of IPV Immunogenicity after Drying without Freezingor Foam Formation

Such samples have not been subjected to stresses associated with thebubbling that accompanies foam formation or freezing. Experiments wereperformed to determine whether this method produced a high level ofantigen retention when used to dry IPV.

Three separate experiments were performed in which IPV was resuspendedin an aqueous solution with 10% sucrose or 10% trehalose as thestabilizing agent. The samples were put into siliconized vials whichwere placed into a Heto Drywinner 8-85 freeze-dryer and the temperaturewas set to 15° C. The pressure was initially reduced to 35 mBars todegas the sample. After 10 minutes, the pressure was further reduced to8 mBars and was kept at this level for two hours. During this period thetemperature setting was kept at 15° C. and the temperature into thesample was monitored. As water evaporated from the sample, thetemperature dropped to 4° C. but towards the end of the two hours, thetemperature returned to 15° C. as the rate of evaporation slowed. Nobubbling or foam formation occurred under these conditions. The pressurewas then reduced further to 0.1 mbars and these conditions weremaintained for 16 hours more in the first two experiments and for 10hours more in the third experiment.

The samples were reconstituted in water and an ELISA was used to assessthe retention of antigenicity of the three polio virus strains. Themonoclonal antibody against type 3 IPV, was used in an ELISA to assessthe degree of antigen retention in the reconstituted, freeze driedsample compared to a reference sample that had not been frozen. Resultsare presented as a percentage of the reading given for a sample whichhad not undergone a drying procedure.

Results

The dried samples had a solid appearance however they appeared to be inthe form of a highly viscous liquid/glass since, over a period of days,the dried sample was able to flow if the container was inverted.

TABLE 2 Retention of type 3 IPV antigen as determined by ELISA using amonoclonal antibody (drying without foaming or freezing) 1^(st)experiment 2^(nd) experiment 3^(rd) experiment Formulation (18 hourcycle) (18 hour cycle) (12 hour cycle) No sugar 0% 2.5% sucrose 0% 10%sucrose 75%  78% 91% 10% trehalose 82%  79% 93%

These levels of type 3 IPV antigen retention compare very favorably withthe freeze drying results shown below where very low values were usuallyfound in the same ELISA format when a monoclonal antibody against type 3was used.

TABLE 3 Retention of type 1, 2 and 3 IPV antigens as determined by ELISAusing a monoclonal and polyclonal antibodies (freeze drying) ELISA -type 1/2/3% Method of drying Polyol content Polyclonal Monoclonal Freezedrying 3.15% sucrose  46/49/58* 19/25/0 Freeze drying 10% trehalose47/43/58 25/0/0  *The experiment freeze drying in the presence of 3.15%sucrose was repeated five times and the results shown are from onerepresentative experiment.

Example 4 Long Term Storage Stability of Dried IPV Stored as a HighlyViscous Liquid/Glass

IPV dried using the method described in Example 3 was stored at 4° C.for 9 months. The samples were reconstituted in water with 150 mM NaCland an ELISA was used to assess the retention of antigenicity of thethree polio virus strains. Three monoclonal antibodies, one against eachstrain, were used in separate ELISAs to assess the degree of antigenretention in the reconstituted stored sample. A similar ELISA had beencarried out on reconstituted samples from the same batch prior tostorage. All results were compared to a reference sample that had notbeen dried. Results are presented as a percentage of the reading givenfor a sample which had not undergone a drying procedure.

Results

TABLE 4 Retention of IPV antigens after storage as a highly viscousliquid for 9 months Treatment Type 1 ELISA Type 2 ELISA Type 3 ELISADried/reconstituted 72% 75% 88% Not stored Dried/reconstituted 70% 94%90% 9 months 4° C.

Therefore IPV which has been dried by the method described in Example 3an be stored at 4° C. for at least 9 months without loss ofantigenicity.

Example 5 Comparison of the Immunogenicity in Vivo of IPV after Dryingto form a Highly Viscous Liquid and Reconstitution Compared to UndriedIPV

Groups of 10 Wistar rats were inoculated with various dilutions of IPVwhich had been dried in the presence of 10% sucrose to form a highlyviscous liquid using the method disclosed in Example 2 andreconstituted. Further groups of 10 Wistar rats were inoculated withreference samples of IPV which had been prepared in the same way butwhich had not been dried.

After 21 days, sera were taken from all the rats and the sera weretested in separate immunoprecipitation assays using Type 1, Type 2 andType 3 polio virus.

Results are shown in Table 5 that contains: a) the number of respondantrats for each IPV dilution, b) the ED50 which is the dose that isrequired to ensure that 50% of the rats seroconvert as assessed by theimmunoprecipitation assay and c) the relative potency of the dried andreconstituted IPV compared to the undried reference IPV.

TABLE 5 Immunogenicity of IPV after drying to form a high viscosityliquid (JLE017/05) and reconstitution compared to an undried referenceIPV (JLE097) undi- Number of respondant RP relative Sample luted 1/1.251/3.125 1/7.81 ED50 potency JLE017/05 Type 1 10 9 6 5 6.37 0.956 Type 26 4 3 3 7.14 0.825 Type 3 6 8 2 1 18.18 1.051 JLE097 Type 1 10 10 10 73.33 1.120 Type 2 8 6 5 2 3.12 0.951 Type 3 7 6 4 1 16.91 1.172Reference Type 1 10 8 4 6.37 Type 2 7 5 2 2.93 Type 3 5 3 0 22.57

JLEO17/05 is a IPV batch that was dried to form a highly viscous liquidand subsequently reconstituted. The JLE097 is the undried reference.

Table 5 shows that the number of respondants inoculated with eachdilution of IPV is similar between the two batches of dried andreconstituted IPV and the undried reference sample. In general, Type 1IPV elicited the best immune response, with Type 2 eliciting an immuneresponse in slightly fewer rats. Type 3 elicited the weakest immuneresponse.

The process of drying to form a highly viscous liquid does not impairthe ability of IPV to elicit immunoprecipitating antibodies in vivo. Arelative potency (RP) reading of 1.0 indicates that the sample elicitsan equivalent response to the reference sample. Both dried samplesproduce RP readings of close to 1.0 for all three types of polio virusindicating the drying process does not effect the ability of the sampleto elicit an immune response.

Example 6 Effect of Drying to Form a Highly Viscose Liquid Using Sucroseor Trehalose as Stabilizing Agent on the Ability of IPV to Elicit anImmunoprecipitating Immune Response In Vivo

Groups of 10 Wistar rats were inoculated with IPV which had been driedin the presence of either 10% sucrose or 10% trehalose as described inExample 2, and then reconstituted. Further groups of 10 Wistar rats wereinoculated with an equivalent amount of IPV that had not been dried, asreference samples.

After 21 days, sera were collected from all rats and animmunoneutralization assay, as described in Example 5 was used to assessthe amount of immunoneutralizing antibody that had been raised againsteach of Type 1, Type 2 and Type 3 polio virus.

Relative potencies were calculated for each sample by comparing theimmune response to that elicited by the undried reference sample.

Results are shown in Table 6.

TABLE 6 Comparison of drying in sucrose and trehalose Relative potencyHumidity in vivo Type 1/ % Karl Duration Lot Number Sugar present Type2/Type 3 Fischer (hours) Jle017 10% trehalose 0.95/0.82/1.05 nd 731CO3/01 10% sucrose 0.69/1.20/0.97 4.6% 18 31CO3/02 10% trehalose0.60/0.94/0.9  11.5% 18 03D02/01 10% sucrose 0.74/1.05/0.96 5.9% 1203D02/02 10% trehalose 0.58/0.98/1.06 10.6% 12

The amount of water remaining in samples was lower when sucrose was usedas stabilizing agent with approximately 5% humidity remaining comparedto approximately 10% when trehalose was used as the stabilizing agentmeasured by a Karl Fischer coulometric moisture analyzer.

Both sucrose and trehalose were effective at stabilizing IPV during thedrying process so that the reconstituted IPV gave relative potencyreadings approaching 1.0 for most of the different types of polio virus.The relative potencies were particularly good for Type 3 polio viruswhich loses its immunogenicity relatively easily.

Example 7 Measurement of Humidity by Karl Fischer

Analysis was carried out in a Karl Fischer titrometer (Aqua30.00—Elektrochemie Halle). The sample was weighed out and placed intothe oven at a setting of 80° C. The sample was flushed with nitrogen gasand then added to hydranal reagent (Riedel de Hahn) in order to performthe analysis by coulometry.

1. A method for preserving an active agent comprising the steps of: a)preparing a preservation sample by dissolving or suspending active agentin a solution of a stabilizing agent comprising a polyol at aconcentration of between 3.15% and 50% (w/v); b) subjecting thepreservation sample to a temperature condition and to a pressurecondition below 30 mbar, such that the preservation sample loses solventby evaporation without freezing or bubbling, thereby forming a viscousliquid, wherein the active agent retains at least 40% of theantigenicity, activity, immunogenicity, or combination thereof, ascompared to a reference sample that has not been subject to theevaporation process.
 2. The method of claim 1, further comprising thestep of: c) further subjecting the preservation sample to temperatureand pressure conditions such that the viscous liquid dries to form ahighly viscous liquid.
 3. The method of claim 1, comprising reducing thepressure to at least 2 mBars and no more than 20 mbars during step b).4. The method of claim 1, wherein the temperature external to thepreservation sample is between 5° C. and 37° C. during step b).
 5. Themethod of claim 2, wherein the temperature external to the preservationsample is between 5° C. and 37° C. during step c).
 6. The method ofclaim 2, wherein the temperature external to the preservation sample ishigher during step c) than it is in step b).
 7. The method of claim 6,wherein the temperature external to the preservation sample is increasedto above 20° C. during step c).
 8. The method of claim 2, wherein thepressure is reduced in step c) compared to the pressure during step b).9. The method of claim 8, wherein the pressure is reduced to 1 mbar orbelow during step c).
 10. The method of claim 1, wherein step b) iscompleted in less than 4 hours.
 11. The method of claim 2, wherein stepsb) and c) are completed in less than 12 hours.
 12. The method of claim1, wherein the stabilizing agent comprises a glass forming polyolselected from the group of: glucose, maltulose, iso-maltulose,lactulose, sucrose, maltose, lactose, sorbitol, iso-maltose, maltitol,lactitol, palatinit, trehalose, raffinose, stachyose, melezitose, anddextran.
 13. The method of claim 12, wherein the stabilizing agent issucrose.
 14. The method of claim 12, wherein the concentration ofstabilizing agent is 5-10% (w/v).
 15. The method of claim 1, wherein thepreservation sample comprises phenol red.
 16. The method of claim 1,wherein the preservation sample is dried in a container with a solventrepellent interior surface.
 17. The method of claim 1, wherein theactive agent comprises a molecule selected from the group of: protein,peptide, amino acid, polynucleotide, oligonucleotide, polysaccharide,oligosaccharide, polysaccharide-protein conjugate, andoligosaccharide-protein conjugate.
 18. The method of claim 1, whereinthe active agent comprises a biological system selected from the groupof: cells, subcellular compositions, bacteria, viruses, virus componentsand virus like particles.
 19. The method of claim 18, wherein the activeagent comprises IPV (inactivated polio virus).
 20. The method of claim18, wherein the active agent comprises Haemophilus influenzae type bpolysaccharide or oligosaccharide.
 21. The method of claim 18, whereinthe active agent comprises Neisseria meningitidis C polysaccharide oroligosaccharide.
 22. The method of claim 1, wherein the active agentcomprises a vaccine.
 23. A composition obtained by the method of claim1, comprising a highly viscous liquid comprising an active agent and aglass forming polyol stabilizing agent wherein the composition comprisesa solvent content of less than 15% (w/w).
 24. The composition of claim23, wherein the active agent retains at least 40% of the antigenicity,activity, inimunogenicity, or combination thereof, as compared to areference sample that has not been subject to the evaporation process.25. The composition of claim 23, comprising a glass forming polyolselected from the group of: glucose, maltulose, iso-maltulose,lactulose, sucrose, maltose, lactose, sorbitol, iso-maltose, maltitol,lactitol, palatinit, trehalose, raffinose, stachyose, melezitose, anddextran.
 26. The composition of claim 25, wherein the glass formingpolyol is sucrose.
 27. The composition of claim 23, wherein the activeagent comprises a molecule selected from the group of: protein, peptide,amino acid, polynucleotide, oligonucleotide, polysaccharide,oligosaccharide, polysaccharide-protein conjugate, andoligosaccharide-protein conjugate.
 28. The composition of claim 23,wherein the active agent comprises a biological system selected from thegroup of: cells, subcellular compositions, bacteria, viruses, viruscomponents, and virus like particles.
 29. The composition of claim 23,wherein the active agent comprises a vaccine.
 30. The composition ofclaim 23, wherein the active agent comprises IPV.
 31. The composition ofclaim 23, wherein the active agent comprises a bacterial polysaccharideor oligosaccharide.
 32. The composition of claim 31, wherein the activeagent comprises a Haemophilus influenzae b polysaccharide oroligosaccharide.
 33. The composition of claim 23, wherein the activeagent comprises a Neisseria meningitidis serogroup C polysaccharide oroligosaccharide.
 34. The composition of claim 23, held within acontainer with a solvent repellent interior surface.
 35. An immunogeniccomposition or vaccine comprising the composition of claim 23, and apharmaceutically acceptable excipient.
 36. A method of making a vaccinecomprising the step of reconstituting the composition of claim 23, in anaqueous solution.
 37. The method of claim 36, wherein the aqueoussolution comprises a mixture of acellular or whole cell Diphtheriaantigen, Tetanus antigen and Pertussis antigens.
 38. The method of claim37,wherein the vaccine comprising the mixture of acellular or whole cellDiphtheria antigen, Tetanus antigen and Pertussis antigens is at leastin part adjuvanted with aluminium hydroxide.
 39. A kit comprising thecomposition of claim 23, held in a first container and a liquid vaccinecomponent held in a second container.
 40. The composition of claim 31,wherein the polysaccharide or oligosaccharide is conjugated to a carrierprotein.
 41. The method of claim 1, wherein the stabilizing agent ispresent at a concentration of between 3.15% and 25% (w/v).